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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920959Generated: October 26, 2026

1-(4-(Bis(4-methoxybenzyl)amino)-2-isobutylimidazo[1,2-a]quinoxalin-1-yl)-2-methylpropan-2-ol → 1-(4-Amino-2-isobutylimidazo[1,2-a]quinoxalin-1-yl)-2-methylpropan-2-ol

https://huagongshe.com/reaction/1920959

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-(Bis(4-methoxybenzyl)amino)-2-isobutylimidazo[1,2-a]quinoxalin-1-yl)-2-methylpropan-2-olHCID 58004769—
SolventTrifluoroacetic acidHCID 6422—
Product1-(4-Amino-2-isobutylimidazo[1,2-a]quinoxalin-1-yl)-2-methylpropan-2-olHCID 2495792477.1%

Reaction Steps

The solution of 1-(4-(bis(4-methoxybenzyl)amino)-2-isobutylimidazo[1,2-a]quinoxalin-1-yl)-2-methylpropan-2-ol (15 mg, 0.027 mmol) in 1 mL of trifluoroacetic acid was stirred at 70° C. for 6 hours. The solvent was removed under reduced pressure. And then 10 mL of saturated aqueous sodium bicarbonate was added. The resulting mixture was extracted with 70 mL of ethyl acetate. The organic layer was separated and then washed with water (15 mL), brine (15 mL), dried over MgSO4, filtered and concentrated. The crude product was purified by preparative TLC sheet (ethyl acetate and hexanes) to give the titled compound (6.5 mg, 77%). MS: MH+=313. 1H NMR (300 MHz, CDCl3): δ 8.41 (dd, 1H), 7.64 (dd, 1H), 7.25-7.41 (m, 2H), 5.63 (brs, 2H), 3.51 (s, 2H), 2.64 (d, 2H), 2.21 (m, 1H), 1.37 (s, 6H), 0.95 (d, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173657B2
Source datasetuspto-grants-2012_05
ORD IDord-a16ab357f2a8440d8118eaa1a5788721
Source noteuspto-grants-2012_05